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Curriculum
Chapter 1
Foundations and Disease Types
Build a solid foundation in cardiac amyloidosis. Understand what amyloid is, how it infiltrates and damages the heart, and learn to classify the major disease types – AL, serum, hereditary ATTR (hATTR), and wild-type ATTR. Explore the epidemiology and true prevalence of amyloid heart disease.
6 lectures and 1 quizzes
Lectures & Quizzes:
Chapter 2
Systemic Clues and Red Flags
Learn to recognize amyloidosis from early on. This chapter walks through red flags regarding systemic symptoms across organ systems that point to amyloidosis, then zooms in on the cardiac signs every echocardiographer should catch early to trigger a timely diagnostic workup.
4 lectures and 1 quizzes
Lectures & Quizzes:
Chapter 3
Imaging and Differentials
Master the echocardiographic hallmarks of cardiac amyloidosis. Explore key 2D and Doppler features, the full spectrum of echo findings from subtle to classic, as well as their patterns on speckle tracking (strain analysis). Learn to differentiate it from hypertrophy of other causes.
5 lectures and 1 quizzes
Lectures & Quizzes:
Chapter 4
Diagnosis to Treatment and What’s Next
We walk you through the diagnostic algorithm. You will learn how to approach the co-occurrence of aortic stenosis and amyloid cardiomyopathy and heart failure management in this unique population. We will review current targeted therapies and the emerging approaches.
5 lectures and 1 quizzes
Lectures & Quizzes:
Objectives
Identify the different types of cardiac amyloidosis—including AL, wild-type ATTR, and hereditary ATTR (hATTR)—and understand their distinct mechanisms, epidemiology, and clinical implications.
Recognize the systemic and cardiac red flags that should raise suspicion for amyloid heart disease and prompt timely diagnostic workup in everyday clinical practice.
Master the key echocardiographic features of cardiac amyloidosis on 2D and Doppler imaging, and confidently differentiate infiltrative disease from other causes of left ventricular hypertrophy.
Apply a structured diagnostic algorithm to confirm cardiac amyloidosis efficiently and navigate complex scenarios such as the overlap between aortic stenosis and amyloid cardiomyopathy.
Manage heart failure in patients with amyloid cardiomyopathy and select appropriate targeted therapies, while staying informed about emerging treatments shaping the future of care.
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